TY - JOUR
T1 - Neuroendocrine and peripheral activities of ghrelin
T2 - Implications in metabolism and obesity
AU - Muccioli, Giampiero
AU - Tschöp, Matthias
AU - Papotti, Mauro
AU - Deghenghi, Romano
AU - Heiman, Mark
AU - Ghigo, Ezio
N1 - Funding Information:
Personal studies reported in this review have been performed with financial support from the Italian Ministry of University and Research, Rome, Italy (“ex-60%” 1997 and 2000, and MM06318538), the National Council for the Research, CNR, Rome, Italy (98.03040.CT04), from Eureka Project (Peptido project 1923), SMEM Foundation and Europeptides, France.
PY - 2002/4/12
Y1 - 2002/4/12
N2 - Ghrelin, a 28-amino acid acylated peptide predominantly produced by the stomach, displays strong growth hormone (GH)-releasing activity mediated by the hypothalamus-pituitary GH secretagogue (GHS)-receptors specific for synthetic GHS. The discovery of ghrelin definitely changes our understanding of GH regulation but it is also already clear that ghrelin is much more than simply a natural GHS. Ghrelin acts also on other central and peripheral receptors and shows other actions including stimulation of lactotroph and corticotroph secretion, orexia, influence on gastro-entero-pancreatic functions, metabolic, cardiovascular and anti-proliferative effects. GHS were born more than 20 years ago as synthetic molecules suggesting the option that GH deficiency could be treated by orally active GHS as an alternative to recombinant human GH (rhGH). Up to now, this has not been the case and also their usefulness as anabolic anti-aging intervention restoring GH/insulin-like growth factor-I axis in somatopause is still unclear. We are now confronted with the theoretical possibility that GHS analogues could become candidate drugs for treatment of pathophysiological conditions in internal medicine totally unrelated to disorders of GH secretion. Particularly, GHS receptor agonists or antagonists acting on appetite could represent new drug intervention in eating disorders.
AB - Ghrelin, a 28-amino acid acylated peptide predominantly produced by the stomach, displays strong growth hormone (GH)-releasing activity mediated by the hypothalamus-pituitary GH secretagogue (GHS)-receptors specific for synthetic GHS. The discovery of ghrelin definitely changes our understanding of GH regulation but it is also already clear that ghrelin is much more than simply a natural GHS. Ghrelin acts also on other central and peripheral receptors and shows other actions including stimulation of lactotroph and corticotroph secretion, orexia, influence on gastro-entero-pancreatic functions, metabolic, cardiovascular and anti-proliferative effects. GHS were born more than 20 years ago as synthetic molecules suggesting the option that GH deficiency could be treated by orally active GHS as an alternative to recombinant human GH (rhGH). Up to now, this has not been the case and also their usefulness as anabolic anti-aging intervention restoring GH/insulin-like growth factor-I axis in somatopause is still unclear. We are now confronted with the theoretical possibility that GHS analogues could become candidate drugs for treatment of pathophysiological conditions in internal medicine totally unrelated to disorders of GH secretion. Particularly, GHS receptor agonists or antagonists acting on appetite could represent new drug intervention in eating disorders.
KW - Food intake, control of
KW - Ghrelin
KW - Growth hormone secretagogue
KW - Metabolic fuel
KW - Obesity
KW - Pituitary hormone
UR - http://www.scopus.com/inward/record.url?scp=0037066587&partnerID=8YFLogxK
U2 - 10.1016/S0014-2999(02)01432-2
DO - 10.1016/S0014-2999(02)01432-2
M3 - Article
C2 - 12007539
AN - SCOPUS:0037066587
SN - 0014-2999
VL - 440
SP - 235
EP - 254
JO - European Journal of Pharmacology
JF - European Journal of Pharmacology
IS - 2-3
ER -